CAT-354 Clinical Update
Cambridge Antibody Tech Group PLC
23 June 2005
FOR IMMEDIATE RELEASE
07.00 BST, 02.00 EST Thursday 23 June 2005
For further information contact: Weber Shandwick Square Mile (Europe)
Cambridge Antibody Technology Tel: +44 (0) 20 7067 0700
Tel: +44 (0) 1223 471 471 Kevin Smith
Peter Chambre, Chief Executive Officer Yvonne Alexander
John Aston, Chief Financial Officer Rachel Taylor
Rowena Gardner, Director of Corporate
Communications BMC Communications/The Trout Group (USA)
Tel: 001 212 477 9007
Brad Miles, ext 17 (media)
Brandon Lewis, ext 15 (investors)
CAMBRIDGE ANTIBODY TECHNOLOGY ANNOUNCES DATA FROM PHASE I CLINICAL TRIAL OF
CAT-354
Cambridge, UK - Cambridge Antibody Technology (LSE: CAT; NASDAQ: CATG) today
announces that preliminary results of a Phase I clinical trial of CAT-354, a
human anti-IL13 monoclonal antibody being studied as a potential treatment for
severe asthma, showed CAT-354 to be well tolerated with no safety concerns
identified.
The objective of the trial, which commenced in September 2004, was to assess the
safety, tolerability and pharmacokinetics of CAT-354. It was a double-blind,
placebo-controlled, rising single dose intravenous study in 34 mild asthmatic
patients. Preliminary results showed that CAT-354 was well tolerated at all
doses and there were no identified safety concerns; pharmacokinetics were as
anticipated. The trial results will be submitted to an appropriate scientific
meeting in due course.
Based on these results, CAT is planning to start a clinical pharmacology study
in the fourth quarter of 2005. This is being planned as a repeat dose allergen
challenge study in patients with asthma.
Patrick Round, VP Development at CAT, commented: "CAT-354 is an important
product candidate for CAT and this trial was the first clinical step in its
development as a potential treatment for severe asthma. We are encouraged by
these preliminary results and are now moving forward with plans for a second
clinical trial."
- ENDS-
Notes To Editors - Cambridge Antibody Technology (CAT):
Business:
- CAT is a leading biopharmaceutical company, committed to
developing fully human monoclonal antibody therapeutics to treat human
diseases in areas of unmet medical need
- CAT has a strong financial position and expects growing revenues from
HUMIRA(R). In addition, CAT has good medium term prospects from 10 further
CAT-derived clinical development programmes and significant opportunities
for growth in the longer term.
Products:
- HUMIRA, licensed to Abbott, is the first CAT-derived antibody to be
approved for marketing. It was isolated and optimised in collaboration
with Abbott and has been approved for marketing as a treatment for
rheumatoid arthritis in 58 countries.
- There are six further CAT-derived antibodies licensed to partners at
various stages of clinical development, including ABT-874 (Abbott),
LymphoStat-B, HGS-ETR1, HGS-ETR2 (all HGSI) and MYO-029 (Wyeth). CAT has
also licensed its proprietary technologies and patents to several companies,
including: Abbott, Amgen, Chugai, Dyax, Genzyme, Human Genome Sciences,
Merck & Co, Micromet, Pfizer and Wyeth Research, and three antibody drug
candidates are in clinical development at IP licensees.
- There is one proprietary CAT human therapeutic antibody product candidate,
CAT-354, in clinical development, with one further product candidate,
GC-1008 (with Genzyme), in pre-clinical development.
Collaborations:
- CAT has a broad collaboration with Genzyme for the development and
commercialisation of antibodies directed against TGFbeta, a family of proteins
associated with fibrosis and scarring, and with potential application in
the treatment of some cancers.
- CAT has major strategic alliance with AstraZeneca to discover and develop
human antibody therapeutics, principally in inflammatory disorders. This
provides CAT with the opportunity to build a substantial pipeline of
antibody therapeutics with a significant pharmaceutical partner.
- CAT has a third co-development collaboration with Amrad.
Science:
- CAT has an advanced proprietary technology for rapidly isolating human
monoclonal antibodies using Phage Display and Ribosome Display systems.
CAT has extensive phage antibody libraries, currently incorporating more
than 100 billion distinct antibodies, which form the basis for the
Company's strategy to develop a portfolio of antibody-based drugs.
Business Background:
- Based near Cambridge, UK, CAT currently employs around 290 people.
- CAT is listed on the London Stock Exchange (CAT) and on NASDAQ (CATG).
- CAT raised £41m in its IPO in March 1997 and £93m in a secondary offering
in March 2000.
- More information can be found at www.cambridgeantibody.com
IL-13 and CAT-354:
- IL-13 is an interleukin (protein) which has potent immunomodulatory
effects. It is primarily secreted by TH2 lymphocytes. It is believed to be
a highly relevant target molecule for asthma as a result of its potential
role in airways obstruction, acute exacerbations and in chronic airways
remodelling.
- CAT-354 is the first CAT antibody optimised using CAT's proprietary
ribosome display technology to enter clinical development.
- CAT-354 is the latest CAT-derived antibody to enter clinical trials.
Application of the Safe Harbor of the Private Securities Litigation Reform Act
of 1995: This press release contains statements about Cambridge Antibody
Technology Group plc ("CAT") that are forward looking statements. All statements
other than statements of historical facts included in this press release may be
forward looking statements within the meaning of Section 21E of the Securities
Exchange Act of 1934. These forward looking statements are based on numerous
assumptions regarding the company's present and future business strategies and
the environment in which the company will operate in the future. Certain factors
that could cause the company's actual results, performance or achievements to
differ materially from those in the forward looking statements include: market
conditions, CAT's ability to enter into and maintain collaborative arrangements,
success of product candidates in clinical trials, regulatory developments and
competition. We caution investors not to place undue reliance on the forward
looking statements contained in this press release. These statements speak only
as of the date of this press release, and we undertake no obligation to update
or revise the statements.
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